MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2020-03-19 for 25GA ILLUMINATED DIRECTIONAL LASER PROBE 55.48.25P manufactured by Bausch + Lomb.
Report Number | 0001932402-2020-00003 |
MDR Report Key | 9856327 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2020-03-19 |
Date of Report | 2020-02-26 |
Date of Event | 2020-02-26 |
Report Date | 2005-01-01 |
Date Reported to FDA | 2005-01-01 |
Date Reported to Mfgr | 2005-01-10 |
Date Mfgr Received | 2020-02-26 |
Date Added to Maude | 2020-03-19 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. JULI MOORE |
Manufacturer Street | 3365 TREE COURT INDUSTRIAL BLV |
Manufacturer City | ST. LOUIS MO 63122 |
Manufacturer Country | US |
Manufacturer Postal | 63122 |
Manufacturer Phone | 6362263220 |
Manufacturer G1 | SYNERGETICS |
Manufacturer Street | 3345 CORPORATE CENTRE DR |
Manufacturer City | O''FALLON MO 63368 |
Manufacturer Country | US |
Manufacturer Postal Code | 63368 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 25GA ILLUMINATED DIRECTIONAL LASER PROBE |
Generic Name | ILLUMINATED DIRECTIONAL LASER PROBE |
Product Code | HQB |
Date Received | 2020-03-19 |
Model Number | 55.48.25P |
Catalog Number | 55.48.25P |
Lot Number | M0025234 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BAUSCH + LOMB |
Manufacturer Address | ROCHESTER NY 14609 US 14609 |
Product Code | --- |
Date Received | 2020-03-19 |
Device Sequence No | 101 |
Device Event Key | 0 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-19 |